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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00435552
Other study ID # C.2007.001
Secondary ID
Status Completed
Phase Phase 1
First received February 14, 2007
Last updated February 14, 2007
Start date February 2007

Study information

Verified date January 2007
Source C.R.Darnall Army Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The application of Ease-it Spray will alleviate pain secondary to fire ant stings more quickly than placebo.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- AD soldier in US Army

- Ages 18-60

- Volunteer

- Absence of serious medical condition

- Past allergic reactions

- Asthma

- History of (h/o) IFA sting

Exclusion Criteria:

- Inability to provide informed consent

- Known h/o hymenoptera allergic reaction

- Allergy to any component of the treatments

- Inability to follow-up

- Active medical condition

- Pregnancy

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Procedure:
Ease-It Spray


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
C.R.Darnall Army Medical Center
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